Expandable stimulation leads and methods of use

ABSTRACT

Devices, systems and methods are provided for stimulating a target tissue, particularly a dorsal root ganglion. The devices and systems have one or more electrodes, wherein the electrodes are positionable in disperse locations within the specific target area. In some embodiments, the position of at least some of the electrodes is adjustable and optionally independently positionable. Some or all of the electrodes may be used to stimulate the desired tissue, such as to stimulate a specific portion of the target area. Or, the one or more electrodes that fall near the target tissue may be used to stimulate the tissue while the other electrodes are not used. When stimulating the dorsal root ganglion, sensory pain signals are blocked providing relief to the patient.

CROSS-REFERENCES TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 11/952,065, filed Dec. 06, 2007 which claims priority of provisional patent application No. 60/873,465 (Attorney Docket No. 10088-705,101), filed on Dec. 6, 2006, which are both incorporated herein by reference for all purposes,

STATEMENT AS TO RIGHTS TO INVENTIONS MADE UNDER FEDERALLY SPONSORED RESEARCH AND DEVELOPMENT

NOT APPLICABLE

REFERENCE TO A “SEQUENCE LISTING,” A TABLE, OR A COMPUTER PROGRAM LISTING APPENDIX SUBMITTED ON A COMPACT DISK

NOT APPLICABLE

BACKGROUND OF THE INVENTION

The application of specific electrical energy to the spinal cord for the purpose of managing pain has been actively practiced since the 1960s. It is known that application of an electrical field to spinal nervous tissue can effectively mask certain types of pain transmitted from regions of the body associated with the stimulated nervous tissue. Such masking is known as paresthesia, a subjective sensation of numbness or tingling in the afflicted bodily regions. Application of electrical energy has been based on the gate control theory of pain, Published in 1965 by Meizack and Wall, this theory states that reception of large nerve fiber information, such as touch, sense of cold, or vibration, would turn off or close the gate to reception of painful small nerve fiber information. The expected end result would, therefore, be pain relief. Based on the gate control theory, electrical stimulation of large fibers of the spinal cord cause small fiber information to be reduced or eliminated at that spinal segment and all other information downstream from that segment would be reduced or eliminated as well. Such electrical stimulation of the spinal cord, once known as dorsal column stimulation, is now referred to as spinal cord stimulation or SCS.

FIGS. 1A-1B illustrate conventional placement of an SCS system 10. Conventional SCS systems include an implantable power source or implantable pulse generator (IPG) 12 and an implantable lead 14. Such PGs 12 are similar in size and weight to pacemakers and are typically implanted in the buttocks of a patient P. Using fluoroscopy, the lead 14 is implanted into the epidural space E of the spinal column and positioned against the dura layer D of the spinal cord S, as illustrated in FIG. 1B. The lead 14 is implanted either through the skin via an epidural needle (for percutaneous leads) or directly and surgically through a mini laminotomy operation (for paddle leads).

FIG. 2 illustrates example conventional paddle leads 16 and percutaneous leads 18. Paddle leads 16 typically have the form of a slab of silicon rubber having one or more electrodes 20 on its surface. Example dimensions of a paddle lead 16 is illustrated in FIG. 3. Percutaneous leads 18 typically have the form of a tube or rod having one or more electrodes 20 extending therearound. Example dimensions of a percutaneous lead 18 is illustrated in FIG. 4.

Implantation of a percutaneous lead 18 typically involves an incision over the low back area (for control of back and leg pain) or over the upper back and neck area (for pain in the arms). An epidural needle is placed through the incision into the epidural space and the lead is advanced and steered over the spinal cord until it reaches the area of the spinal cord that, when electrically stimulated, produces a comfortable tingling sensation (paresthesia) that covers the patient's painful area. To locate this area, the lead is moved and turned on and off while the patient provides feedback about stimulation coverage. Because the patient participates in this operation and directs the operator to the correct area of the spinal cord, the procedure is performed with local anesthesia

Implantation of paddle leads 16 typically involves performing a mini laminotomy to implant the lead. An incision is made either slightly below or above the spinal cord segment to be stimulated. The epidural space is entered directly through the hole in the bone and a paddle lead 16 is placed over the area to stimulate the spinal cord. The target area for stimulation usually has been located before this procedure during a spinal cord stimulation trial with percutaneous leads 18.

Although such SCS systems have effectively relieved pain in some patients, these systems have a number of drawbacks. To begin, as illustrated in FIG. 5, the lead 14 is positioned upon the spinal cord dura layer D so that the electrodes 20 stimulate a wide portion of the spinal cord and associated spinal nervous tissue. The spinal cord is a continuous body and three spinal levels of the spinal cord are illustrated. For purposes of illustration, spinal levels are sub-sections of the spinal cord S depicting that portion where the dorsal root DR and ventral root VR join the spinal cord S. The peripheral nerve N divides into the dorsal root DR and the dorsal root ganglion DRO and the ventral nerve root VR each of which feed into the spinal cord S. An ascending pathway 17 is illustrated between level 2 and level 1 and a descending pathway 19 is illustrated from level 2 to level 3. Spinal levels can correspond to the vertebral levels of the spine commonly used to describe the vertebral bodies of the spine. For simplicity, each level illustrates the nerves of only one side and a normal anatomical configuration would have similar nerves illustrated in the side of the spinal cord directly adjacent the lead.

Motor spinal nervous tissue, or nervous tissue from ventral nerve roots, transmits muscle/motor control signals. Sensory spinal nervous tissue, or nervous tissue from dorsal nerve roots, transmit pain signals. Corresponding dorsal and ventral nerve roots depart the spinal cord “separately”; however, immediately thereafter, the nervous tissue of the dorsal and ventral nerve roots are mixed, or intertwined. Accordingly, electrical stimulation by the lead 14 often causes undesirable stimulation of the motor nerves in addition to the sensory spinal nervous tissue.

Because the electrodes span several levels the generated stimulation energy 15 stimulates or is applied to more than one type of nerve tissue on more than one level. Moreover, these and other conventional, non-specific stimulation systems also apply stimulation energy to the spinal cord and to other neural tissue beyond the intended stimulation targets. As used herein, non-specific stimulation refers to the fact that the stimulation energy is provided to all spinal levels including the nerves and the spinal cord generally and indiscriminately. Even if the epidural electrode is reduced in size to simply stimulate only one level, that electrode will apply stimulation energy indiscriminately to everything (i.e. all nerve fibers and other tissues) within the range of the applied energy. Moreover, larger epidural electrode arrays may alter cerebral spinal fluid flow thus further altering local neural excitability states.

Another challenge confronting conventional neurostimulation systems is that since epidural electrodes must apply energy across a wide variety of tissues and fluids (Le. CSF fluid amount varies along the spine as does pia mater thickness) the amount of stimulation energy needed to provide the desired amount of neurostimulation is difficult to precisely control. As such, increasing amounts of energy may be required to ensure sufficient stimulation energy reaches the desired stimulation area. However, as applied stimulation energy increases so too increases the likelihood of deleterious damage or stimulation of surrounding tissue, structures or neural pathways.

Improved stimulation systems and methods are desired that enable more precise and effective delivery of stimulation energy. In particular, systems and methods which deliver stimulation energy to specific target tissue while minimizing delivery to tissue nearby. Such systems should be easily deliverable and accommodate various anatomies. At least some of these objectives will be met by the present invention.

BRIEF SUMMARY OF THE INVENTION

The present invention provides devices, systems and methods for stimulating a target tissue, particularly a target tissue which is small, not easily locatable or benefits from precise stimulation while minimizing stimulation of nearby tissues. An example of such a target tissue is a dorsal root, particularly a dorsal root ganglion (DRG), of a spinal anatomy. The dorsal root (or posterior root) is the afferent sensory root of a spinal nerve. Along the dorsal root is the DRG, which contains the neuron cell bodies of the nerve fibers conveyed by the root. Stimulation of the ORG itself blocks sensory pain signals providing relief to the patient. It is desired to focus stimulation onto the ORG while minimizing stimulation of surrounding tissue, particularly nearby spinal anatomy such as the ventral root which carries motor neurons. By focusing such stimulation, pain may be treated with minimal or no adverse affect on motor sensations. In order to most effectively stimulate the DRG while minimizing or excluding undesired stimulation of other anatomies, it may be desired to position a stimulation electrode as dose as possible to the DRG (such as within 1 mm). This may be challenging when the exact location of the DRG is unknown or difficult to reach.

Specific DRGs may be challenging to locate in certain patients or under certain conditions. The DRG is surrounded by the bony anatomy of the vertebrae and is accessible via the spinal column or laterally through a foramen. Each approach involves careful navigation through the anatomy. The anatomies of both the vertebrae and the spinal tissue may vary from patient to patient and from spinal level to spinal level based on both natural variation and previous injury or disease progression. Such variation may impede easy and direct access to the DRG. Further, the ORG is a relatively small target which may be difficult to locate amidst its surrounding tissue. Thus, in some instances the exact location of the DRG may be unknown.

The devices, systems and methods of the present invention assist in stimulating such target tissues while minimizing stimulation of undesired non-target tissues. It may be appreciated that although the following examples are described and illustrated in relation to the DRG, the present invention may be used to stimulate any target tissue within the spinal anatomy, such as the dorsal root or the ventral root, or elsewhere in the general anatomy.

In a first aspect of the present invention, lead devices and systems are provided having one or more electrodes, wherein the electrodes are positionable in disperse locations within a specific target area. In some embodiments, at least some of the electrodes are independently positionable. And, in some embodiments, the position of at least some of the electrodes is adjustable. Some or all of the electrodes may be used to stimulate the desired tissue, such as to stimulate a specific portion of the target area. Or, the one or more electrodes that fall near the target tissue may be used to stimulate the tissue while the other electrodes are not used.

In a second aspect of the present invention, methods are provided for stimulating a target tissue. In some embodiments, such methods include advancing a shaft toward the target tissue, extending at least two electrode shafts from the shaft, wherein each electrode shaft has an electrode, positioning each electrode in proximity to the target tissue, and energizing at least one of the electrodes to stimulate the target tissue.

In preferred embodiments, the target tissue comprises a dorsal root ganglion. In some embodiments, energizing includes energizing a minimum number of electrodes to stimulate the dorsal root ganglion and not energizing remaining electrodes. Likewise, in some embodiments, energizing includes energizing at least one electrode positioned near the dorsal root ganglion and not energizing at least one other electrode positioned further way from the dorsal root ganglion.

Extending at least two electrode shafts from the shaft may include extending at least one of the electrode shafts radially outwardly from the shaft. In some instances, extending includes extending the at least Iwo electrode shafts in directions at least 45 degrees apart. Or, extending may include extending the at least two electrode shafts in directions at least 90 degrees apart. Optionally, extending includes extending a plurality of electrode shafts in a circular configuration radially outwardly from the shaft.

The at least two electrode shafts may be extended through separate lumens in the shaft. Or, at least some of the at least two electrode shafts may be extended through a common lumen in the shaft. In some embodiments, positioning includes steering each electrode shaft. Optionally, positioning includes independently positioning each electrode shaft.

When approaching the target tissue, particularly a dorsal root ganglion, advancing may include advancing the shaft through an epidural space. Or, advancing may include approaching the dorsal root ganglion from outside of a spinal column. In such instances, advancing may include advancing the shaft at least partially through a foramen.

In another aspect of the present invention, a lead is provided comprising a shaft having a distal end split into at least two finger portions, wherein the finger portions are movable radially outwardly from the shaft, and an electrode disposed on each finger portion. Typically, the at least two finger portions are alignable with a longitudinal axis of the shaft. In some embodiments, at least one finger portion is able to move radially outwardly, such as by recoil due to precurvature. In such embodiments, the lead may further comprise a sheath positionable at least partially over the distal end of the shaft so as to hold the at least two finger portions in alignment with the longitudinal axis and retractable to release the at least one precurved finger portion allowing recoil, Alternatively, the at least one finger portion includes a pull-wire to move radially outwardly. Optionally, the at least one finger portion is independently movable. The at least one finger portion may have a variety of shapes, including a pointed shape. Typically, the shaft includes a central lumen for the passage of tools and other devices.

In some embodiments, the shaft is configured for positioning at least one of the electrodes in proximity to a dorsal root ganglion. Optionally, the shaft may be configured for advancement through an epidural space. Additionally or alternatively, the shaft may be configured for advancement at least partially through a foramen.

In yet another aspect of the present invention, a system is provided comprising a shaft having a distal end split into at least two finger portions, wherein each finger portion has an electrode and each finger portions is movable radially outwardly from the shaft, and a first sheath positionable over the shaft so as to hold each finger portion in alignment with a longitudinal axis. In some embodiments, the first sheath is positionable so as to allow at least one finger portion to move radially outwardly from the shaft while maintaining another finger portion in longitudinal alignment. For example, the first sheath may have an angled distal end. Additionally or alternatively, the first sheath may have a cutout which allows the at least one finger portion to move radially outwardly from the shaft therethrough. Optionally, the system may include a second sheath positionable over the first sheath so as to retrain at least one finger portion.

Other objects and advantages of the present invention will become apparent from the detailed description to follow, together with the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A-1B, 2, 3, 4, 5 illustrate prior art

FIGS. 6A-6B illustrate a lead of the present invention having a shaft and a plurality of electrode shafts, each having at least one electrode, wherein the lead is positioned near the DRG.

FIGS. 7A-7B illustrate an embodiment of a lead of the present invention having three advanceable electrode shafts.

FIG. 8A illustrates an embodiment of the present invention having a plurality of electrode shafts extending through a common lumen,

FIGS. 8B-8C illustrate embodiments of shafts having common lumens for the passage of electrode shafts therethrough.

FIGS. 9A-9B illustrate an embodiment of a lead having a shaft having a distal end split into at least two finger portions.

FIGS. 10A-10B illustrate an alternative embodiment of a lead having a shaft having a distal end split into at least two finger portions.

FIG. 10C illustrates a lead of the present invention including a sheath having an angled distal end.

FIG. 10D illustrates a lead of the present invention including a sheath having a cutout.

DETAILED DESCRIPTION OF THE INVENTION

As mentioned previously, the examples provided herein illustrate the dorsal root ganglion (DRG) as the target tissue, however it may be appreciated that the present invention may be used to stimulate any target tissue within the spinal anatomy or general anatomy. In some instances the target tissue may be adjacent to or in very close proximity to other tissue of which stimulation is to be avoided or reduced. For example, FIGS. 6A-6B provide a histological cross-sectional illustration of spinal anatomy in which the ORG (target tissue) is adjacent to the ventral root VR (non-targeted tissue). A lead 300 of the present invention is shown accessing the ORG via a retrograde spinal column approach. The lead 300 has a shaft 302 and a plurality of electrode shafts 304 a, 304 b, 304 c, each having at least one electrode 306 (typically positioned near its tip), which are extendable from the shaft 302. As shown in FIG. 6A, the lead 300 is typically advanced toward the target tissue with the electrode shafts 304 a, 304 b, 304 c retracted therein. Once the shaft 302 is desirably positioned, the electrode shafts 304 a, 304 b, 304 c are extended, as illustrated in FIG. 6B.

hi the extended or expanded position, the electrodes 306 are positioned in disperse locations within a specific target area (e.g. in, on, around or near the DRG). The position of the electrodes 306 may be adjusted, independently or together, such as by advancement or retraction of the electrode shafts 304. In some embodiments, the electrode shafts 304 are precurved so that their tips disperse, expanding radially outwardly, as illustrated. Optionally, the electrode shafts 304 may be steerable.

In the example of FIG. 6B, although the plurality of electrode shafts 304 a, 304 b, 304 c extend from the shaft 302, only the electrode 306 of electrode shaft 304 b actually contacts the target tissue, the DRG. The electrode 306 of electrode shaft 304 a falls outside of the DRG and the electrode 306 of electrode shaft 304 c contacts the ventral root VR. In this instance, stimulation energy may be applied to the electrode 306 of the electrode shaft 304 b and not to the electrode 306 of the electrode shaft 304 c. This would provide specific stimulation to the DRG (so as to manage pain) while minimizing any stimulation to the ventral root VR (so as to avoid a motor response). Likewise, stimulation energy may not be applied to electrode 306 of electrode shaft 304 a so as to conserve energy. Such a stimulation pattern may be particularly useful in embodiments wherein the electrode shafts move together. In embodiments wherein the electrode shafts move independently, electrode shaft 304 a and electrode shaft 304 c may be removed.

Thus, stimulation may be applied to the target area by supplying electrical energy to all of the electrodes 306 or to a subset of the electrodes 306. In this manner, an area of tissue surrounding the disperse electrodes 306 may be stimulated. In many instances, the location of the electrode shafts 304 and/or electrodes 306 upon delivery are not visible to the practitioner. Thus, the practitioner is unaware as to which electrodes 306 are disposed closest to the target tissue. In such instances, electrical energy may be supplied to the electrodes 306 individually or in groups until the desired effect is achieved. For example, the patient's pain level may be evaluated by stimulation via each of the electrodes 306 individually or in groups, and only the electrodes 306 which provide the desired response will be used for stimulation. These are likely but not necessarily the one or more electrodes 306 which are positioned closest to the DRG.

It may be appreciated that the shaft 302 is advanced toward the DRG by any suitable approach, Embodiments of these approaches may include passing through, near or along one or more posterior or lateral openings in the bony structure of the spinal column. An example of a posterior opening is an opening between adjacent spinous processes. An example of a lateral opening is the foramen or opening at least partially defined by the articulating processes and the vertebrae. In particular, the shaft 302 may be advanced by a retrograde, antegrade or lateral approach to the dorsal root and DRG from the spinal column, such as a transiaminar approach. Alternatively, the shaft 302 may be advanced by a retrograde, antegrade or lateral approach to the dorsal root and DRG from outside of the spinal column, such as from a side or traditional percutaneous approach or a transforamenal approach. In further examples, the shaft 32 may be advanced to the dorsal root and DRG via an antegrade or retrograde approach between an articulating process and the vertebral body. The leads of the present invention may also be positioned by any other suitable method or approach.

FIGS. 7A-7B illustrate an example embodiment of a lead 300 of the present invention. In this embodiment, the lead 300 comprises a shaft 302 having a plurality of internal lumens 310. In this example, three lumens 310 are depicted, however more or less lumens 310 may be present, such as one, two, four, five, six or more lumens 310. In this embodiment, an electrode shaft 304 is extendable through each of the lumens 310, as illustrated in FIG. 7B. In this embodiment, an electrode 306 is disposed near each tip 308 and each electrode 306 is electrically connected to a conductive wire (not shown) which extends along the length of the shaft 302 and connects with a remotely implanted IPG. In this embodiment, the electrode shafts 304 are precurved so that the tips 308 disperse, expanding radially outwardly as shown, during advancement of the electrode shafts 304 through the lumens 310. It may be appreciated that the electrode shafts may extend in various directions, including 15, 30, 45, 90, 120, 180 degrees apart, to name a few. It may also be appreciated that the shafts 304 may alternatively curve inwardly or in any other desired pattern.

The electrode shafts 304 may be comprised of any suitable material, including a polymer, memory metal or spring metal, to name a few. Alternatively or in addition, the electrode shafts 304 may be steerable. Likewise, one or more of the electrode shafts 304 may be independently positionable and/or steerable. Further, one or more the electrode shafts 304 may be independently advanceable and retractable. Once the position of the electrode shafts 304 are optionally adjusted and desirably placed, the shafts 304 may be fixed in place in relation to the shaft 302 and optionally each other.

FIG. 8A illustrates another embodiment of a lead 300 of the present invention. The lead 300 comprises a shaft 302 and a plurality of electrode shafts 304 extending therefrom. The shaft 302 may have a variety of configurations, including a large central lumen 312, as illustrated in FIG. 8B. The electrode shafts 304 pass through the central lumen 312 and extend therefrom, FIG. 8C illustrates an alternative embodiment wherein the shaft 302 comprises a ring lumen 314 surrounding an axial lumen 316. The electrode shafts 304 pass through the ring lumen 314 and extend therefrom. This allows other tools or devices to be passed through the axial lumen 316. Thus, in each of these embodiments the electrode shafts 304 extend through a common lumen.

Referring back to FIG. 8A, twelve electrode shafts 304 are shown, however more or less shafts 304 may extend therethrough depending on the size of the shaft 302 and lumens. An electrode 306 is disposed near each tip 308 of the electrode shafts 304. In this embodiment, the electrode shafts 304 are precurved so that as the electrode shafts 304 advance, shafts 304 expand radially outwardly dispersing the tips 308. Alternatively, the shaft 302 may be retracted, exposing the electrode shafts 304 and allowing the unrestrained shafts 304 to expand radially outwardly. In this embodiment, the plurality of electrode shafts 304 extend in a circular configuration radially outwardly from the shaft 302. Again, once the position of the electrode shafts 304 are optionally adjusted and desirably placed, the electrode shafts 304 may be fixed in place in relation to the shaft 302 and optionally each other.

FIGS. 9A-9B illustrate another embodiment of a lead 300 of the present invention. In this embodiment, the lead 300 has a shaft 302 comprising a split distal end 320. Here, shaft 302 is comprised of a flexible material (such as a flexible polymer or metal), and the distal end 320 is cut so as to create at least two finger portions 322. Thus, the shaft 302 includes a central lumen 326 which may be used for advancement of tools or devices, such as a stylet, therethrough. An electrode 306 is positioned near the tip of each finger portion 322. In this embodiment, the electrodes 306 are disposed on an outside surface of the finger portions 322. However the electrodes 306 may alternatively be positioned on an inside surface or along a distal cross-section. It may be appreciated that more than one electrode may be disposed on each finger portion 322, such as an electrode array. Each electrode 306 is electrically connected with a conductive wire 324 which extends along the shaft 302 and connects with an IPG to provide electrical signals to the associated electrode.

FIG. 9A illustrates the finger portions 322 aligned with a longitudinal axis 323. FIG. 9B illustrates the finger portions 322 expanded radially outwardly from the longitudinal axis 323 so that the electrodes 306 are dispersed. Such expansion may be achieved by a variety of features. For example, each finger portion 322 may be precurved radially outwardly. Such precurvature may be achieved by heat-setting of a polymer or embedding a shape-memory wire or ribbon into each finger portion 322. The finger portions 322 are capable of being held in a restrained position by an outer sheath. Retraction of the outer sheath releases the finger portions 322 and allows the precurvature to draw the finger portions 322 radially outwardly by recoil.

Alternatively, each finger portion 322 may include a pull-wire. wherein applying tension to the pull-wires draws the finger portions 322 radially outwardly. In some embodiments, the position of the finger portions 322 may be adjusted independently by applying tension to the pull-wires independently.

FIGS. 10A-10D illustrate another embodiment of a lead 300 having a shaft 302 comprising a split distal end 320 creating at least two finger portions 322. In this embodiment, the shaft 302 is formed from a nitinol tube covered by an insulated braided wire [WHY?]. In this embodiment, the finger portions 322 have sharp tips upon which the electrodes 306 are plated. Each electrode 306 is electrically connected with a conductive wire 324 which extends along the shaft 302 and connects with an IPG to provide electrical signals to the associated electrode. FIG. 10B illustrates the finger portions 322 expanded radially outwardly so that the electrodes 306 are dispersed. Such expansion is achieved due to shape memory of the nitinol tube. As shown, the shaft 302 includes a central lumen 326 which may be used for advancement of tools or devices, such as a stylet, therethrough.

Typically, the finger portions 322 would be covered with a sheath 330 that is removable to allow expansion of the finger portions 322. Optionally, the sheath 330 may be angled, as illustrated in FIG. 10C, to allow preferential expansion. As shown, the angled sheath 330 covers some of the finger portions 322, holding them in a restrained, unexpanded state, while revealing some of the finger portions 322, allowing them to expand radially outwardly. The proportion of expansion depends on the angle of the sheath 330 and on the radius of curvature of the finger portions 322.

Additionally or alternatively, multiple sheaths may be used with cutouts for each finger portion 322 to allow even more preferential expansion options. For example, FIG. 10D illustrates an embodiment having a first sheath 330 a and a second sheath 330 b. The first sheath 330 a has a tube shape and is capable of restraining all of the finger portions 322 when positioned over the finger portions 332. The second sheath 330 b has a cutout 332 near its distal end. When the first sheath 330 a is retracted, as shown in FIG. 10D, restraint of the finger portions 322 is maintained by the second sheath 330 b in all areas except in the area of the cutout 332 which allows the revealed finger portion 332′ to expand radially outwardly. The second sheath 330 b may be rotated to reveal any desired finger portions (s). It may be appreciated that the sheaths 330 a, 330 b are coaxial and may be layered in any order. It may also be appreciated that the sheaths 330 of FIGS. 10C-10D may be used with any leads 300 of the present invention.

In some embodiments, the leads of the present invention are passable through a 16 gauge needle, 17 gauge needle, 18 gauge needle or a smaller needle. However, in some embodiments, such leads may be passable through a 14-15 gauge needle or a larger needle. In some embodiments, the electrode(s) of the present invention have a less than 2 mm square area, or in some embodiments an approximately 0.6-1 mm square area.

In embodiments having reduced dimensions in electrode area and overall size (e.g. outer diameter), such reductions are possible due to increased specificity of the stimulation energy. By positioning at least one of the electrodes on, near or about the dorsal root ganglion, the stimulation energy is supplied directly to the target anatomy (i.e. the DRG). Thus, a lower power may be used than with a leads which is positioned at a greater distance from the target anatomy. For example, the peak power output of the leads of the present invention are typically in the range of approximately 20 .mu.W-0.5 mW. Such reduction in power requirement for the leads of the present invention in turn may eliminate the need to recharge the power source in the implanted pulse generator (IPG). Moreover, the proximity to the stimulation site also reduce the total amount of energy required to produce an action potential, thus decreasing the time-averaged power significantly and extending battery life.

The above described leads of the present invention may be used with or without the assistance of visualization during the implantation procedure. However, in instances wherein visualization is desired, some embodiments of the lead include means for delivering contrast agent to the target tissue area to assist in visualization via fluoroscopy or other imaging methods. For example, in the embodiment illustrated in FIGS. 7A-7B, the shaft 302 may include an additional lumen through which contrast agent is injected. Or, the electrode shafts 304 may be sized so as to allow simultaneous passage of contrast agent through one or more of the lumens 310. Or, the electrode shafts 304 may include a lumen for passage of contrast agent therethrough. The different types of tissue, such a muscle and nerve, may provide contrast differences that may assist in positioning the lead in a desired location.

Any of the above described devices and systems may be adapted for delivery of a drug or therapeutic agent to a desired target tissue site. Rather than electrodes, hollow tubes may be used. The tubes may be positioned in dispersed locations with a specific target area. Some or all of the tubes may be used to deliver the therapeutic agent to the desired tissue. Or the one or more tubes that fall near the target tissue may be used to delivery the therapeutic agent to the tissue while the other tubes are not used.

Although the foregoing invention has been described in some detail by way of illustration and example, for purposes of clarity of understanding, it will be obvious that various alternatives, modifications and equivalents may be used and the above description should not be taken as limiting in scope of the invention. 

1. A method of stimulating a dorsal root ganglion comprising: advancing a shaft toward the dorsal root ganglion; extending at least two electrode shafts from the shaft, wherein each electrode shaft has an electrode; positioning each electrode in proximity to the dorsal root ganglion; and energizing at least one of the electrodes to stimulate the dorsal root ganglion.
 2. A method as in claim 1, wherein energizing includes energizing a minimum number of electrodes to stimulate the dorsal root ganglion and not energizing remaining electrodes.
 3. A method as in claim 1, wherein energizing includes energizing at least one electrode positioned near the dorsal root ganglion and not energizing at least one other electrode positioned further way from the dorsal root ganglion.
 4. A method as in claim 1, wherein extending includes extending at least one of the electrode shafts radially outwardly from the shaft.
 5. A method as in claim 1, wherein extending includes extending the at least two electrode shafts in directions at least 45 degrees apart.
 6. A method as in claim 5, wherein extending includes extending the at least two electrode shafts in directions at least 90 degrees apart.
 7. A method as in claim 1, wherein extending includes extending a plurality of electrode shafts in a circular configuration radially outwardly from the shaft.
 8. A method as in claim 1, wherein extending includes extending the at least two electrode shafts through separate lumens in the shaft.
 9. A method as in claim 1, wherein extending includes extending at least some of the at least two electrode shafts through a common lumen in the shaft.
 10. A method as in claim 1, wherein advancing includes advancing the shaft through an epidural space.
 11. A method as in claim 1, wherein advancing includes approaching the dorsal root ganglion from outside of a spinal column.
 12. A method as in claim 11, wherein advancing includes advancing the shaft at least partially through a foramen.
 13. A method as in claim 1, wherein positioning includes steering each electrode shaft.
 14. A method as in claim 1, wherein positioning includes independently positioning each electrode shaft.
 15. A lead comprising: a shaft having a distal end split into at least two finger portions, wherein the finger portions are movable radially outwardly from the shaft: and an electrode disposed on each finger portion,
 16. A lead as in claim 15, wherein the at least two finger portions are alignable with a longitudinal axis of the shaft.
 17. A lead as in claim 16, wherein at least one finger portion is precurved so as to move radially outwardly by recoil.
 18. A lead as in claim 17, further comprising: a sheath positionable at least partially over the distal end of the shaft so as to hold the at least two finger portions in alignment with the longitudinal axis and retractable to release the at least one precurved finger portion allowing recoil.
 19. A lead as in claim 15, wherein at least one finger portion includes a pull-wire.
 20. A lead as in claim 15, wherein at least one finger portion is independently movable. 